Matches in Nanopublications for { ?s ?p "[A screen of a pool of 81 healthy, unrelated individuals showed no presence for the homozygous form of this allele, suggesting that NFATC1 is a potential VSD-susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_assertion description "[A screen of a pool of 81 healthy, unrelated individuals showed no presence for the homozygous form of this allele, suggesting that NFATC1 is a potential VSD-susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP337602.RADiO_O6cGMgK8352p7sdoSRqVCA0fKgOdPkUt8vWbR_E130_provenance.
- NP579851.RAeHIL-eojrzmk4V3txi_OwLM64UjfX0Z_-2XnA8UJosk130_assertion description "[A screen of a pool of 81 healthy, unrelated individuals showed no presence for the homozygous form of this allele, suggesting that NFATC1 is a potential VSD-susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP579851.RAeHIL-eojrzmk4V3txi_OwLM64UjfX0Z_-2XnA8UJosk130_provenance.
- NP588714.RA78V4G2dzQibQSsUT5xLiTKursW-IM9yxkN2nEJoejaw130_assertion description "[A screen of a pool of 81 healthy, unrelated individuals showed no presence for the homozygous form of this allele, suggesting that NFATC1 is a potential VSD-susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588714.RA78V4G2dzQibQSsUT5xLiTKursW-IM9yxkN2nEJoejaw130_provenance.